loratadine

Generic: loratadine

Labeler: chain drug marketing association inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loratadine
Generic Name loratadine
Labeler chain drug marketing association inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
Chain Drug Marketing Association Inc.

Identifiers & Regulatory

Product NDC 63868-151
Product ID 63868-151_08f2bf78-eba5-41ce-bcb0-733e2760d44b
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA076134
Listing Expiration 2026-12-31
Marketing Start 2003-08-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63868151
Hyphenated Format 63868-151

Supplemental Identifiers

RxCUI
311372
UNII
7AJO3BO7QN

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name loratadine (source: ndc)
Generic Name loratadine (source: ndc)
Application Number ANDA076134 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (63868-151-01)
  • 10 TABLET in 1 BLISTER PACK (63868-151-10)
  • 30 TABLET in 1 BLISTER PACK (63868-151-30)
source: ndc

Packages (3)

63868-151-01 100 TABLET in 1 BOTTLE (63868-151-01) 63868-151-10 10 TABLET in 1 BLISTER PACK (63868-151-10) 63868-151-30 30 TABLET in 1 BLISTER PACK (63868-151-30)

Ingredients (1)

loratadine (10 mg/1)

Linked Drug Pages (1)

Loratadine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "08f2bf78-eba5-41ce-bcb0-733e2760d44b", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["b4edf5b1-398d-405a-8a42-76044b31ebb7"], "manufacturer_name": ["Chain Drug Marketing Association Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63868-151-01)", "package_ndc": "63868-151-01", "marketing_start_date": "20030819"}, {"sample": false, "description": "10 TABLET in 1 BLISTER PACK (63868-151-10)", "package_ndc": "63868-151-10", "marketing_start_date": "20030819"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (63868-151-30)", "package_ndc": "63868-151-30", "marketing_start_date": "20030819"}], "brand_name": "Loratadine", "product_id": "63868-151_08f2bf78-eba5-41ce-bcb0-733e2760d44b", "dosage_form": "TABLET", "product_ndc": "63868-151", "generic_name": "Loratadine", "labeler_name": "Chain Drug Marketing Association Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA076134", "marketing_category": "ANDA", "marketing_start_date": "20030819", "listing_expiration_date": "20261231"}